Taiwan FDA registration 099e35a7da0e87bb3cf076cc92b58936
"Goyo" manual osteologic surgical instrument (unsterilized)
TW: "五洋" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·HEFEI WUYANG MEDICAL INSTRUMENT CO., LTD.·Registered Dec 12, 2019 – Dec 12, 2024ExpiredRegistration details
- Analysis ID
- 099e35a7da0e87bb3cf076cc92b58936
- Customs Code
- DHA09600403900
Company information
- Manufacturer
- HEFEI WUYANG MEDICAL INSTRUMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- A-SPINE Asia Co., Ltd.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 12, 2019
- Expiry Date
- Dec 12, 2024
About this record
Access comprehensive regulatory information for "Goyo" manual osteologic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 099e35a7da0e87bb3cf076cc92b58936 and manufactured by HEFEI WUYANG MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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